Water Environment Research • 1–10, 2019
RESEARCH ARTICLE
1
Interdisciplinary Center of Marine
and Environmental Research (CIIMAR/
CIMAR), University of Porto, Matosinhos,
Portugal
2
Institut des Sciences Analytiques et de
Physicochimie Pour l’environnement et les
Matériaux, UMR5254, CNRS/ University of
Pau & Pays Adour/ E2S UPPA, Pau, France
3
Department Analytical Chemistry, Science
& Technology Faculty, University of Basque
Country, UPV/EHU, Bilbao, Spain
4
Science Faculty, University of Porto, Porto,
Portugal
Received 17 July 2019; Revised 24
September 2019; Accepted 7 October 2019
Foundation for Science and Technology
(Portugal); European Regional
Development Fund (ERDF), Grant/Award
Number: PT2020
Additional Supporting Information may be
found in the online version of this article.
Correspondence to: Teodor Stoichev,
Interdisciplinary Center of Marine and
Environmental Research (CIIMAR/CIMAR),
University of Porto, Terminal de Cruzeiros
de Leixões, Matosinhos, Portugal.
Email: tstoichevbg@yahoo.com
Robert Duran, Institut des sciences
analytiques et de physicochimie pour
l’environnement et les matériaux,
UMR5254, CNRS/University of Pau & Pays
Adour/E2S UPPA, Pau, France.
Email: robert.duran@univ-pau.fr
DOI: 10.1002/wer.1255
© 2019 Water Environment Federation
Modeling phaeopigment concentrations in water from
a shallow mesotrophic lagoon
Teodor Stoichev ,
1
Robert Duran ,
2
Alberto de Diego ,
3
Vitor M. Vasconcelos
1,4
• Abstract
Concentrations of phaeopigments (Pha) and chlorophyll a (Chl) were determined in
surface waters from a temperate lagoon during six sampling campaigns at high and at
low tide. In order to develop models for phaeopigment concentration in water, it was
necessary to replace Chl with photosynthetic pigment concentration (P
t
= Pha+Chl)
as one of the explanatory variables. Under first approximation, food availability and
water temperature (T) could be considered as independent variables. The concentra-
tions of Pha were then determined following seasonal change of response curves of
the consumer community on T. However, multiple regression models with P
t
, T and,
eventually, salinity as explanatory variables were better able to depict Pha. All equa-
tions, developed with P
t
, were also solved using Chl as an input variable. Although
part of the performance was lost, such back-transformed models can be used at low/
medium T and moderate to high concentrations of Chl. The developed equations
about middle to long-term variations of Pha could be applied to study the biogeo-
chemistry of contaminants related to Pha and to evaluate the dependence on tem-
perature of phytoplankton utilization by consumers. © 2019 Water Environment Federation
• Practitioner points
• Phaeopigment concentration depicted by chlorophyll (Chl), temperature (T), and
salinity.
• Better results obtained at low to medium T and moderate to high Chl concentration.
• Multiple regression (MR) better for extrapolation than model (S) with variable
separation.
• Thermal response of consumer community in mesotrophic lagoon studied using model S.
• Key words
coastal lagoons; modeling; phaeopigments; phytoplankton; zooplankton
Introduction
The level of chlorophyll a (Chl) in water is a widely used indicator for phyto-
plankton biomass. The concentration in water of the decomposition products of
Chl—the phaeopigments (Pha), is related to a variety of aquatic biogeochemical
processes, for example, phytoplankton decay. Consequently, it may reflect higher
dissolved organic matter concentrations in estuaries (Luengen & Flegal, 2009;
Viličić, Legović, & Žutić, 1989) and seas (Maciejewska & Pempkowiak, 2015). Both
Chl and Pha were used as predictors of estuarine copepod density, diversity, and
dynamics (Islam, Ueda, & Tanaka, 2006). Pattern of Pha in water is indicative of
herbivorous zooplankton grazing in a variety of coastal environments: a shallow
temperate estuary (Biancalana, Menéndez, Berasategui, Fernández-Severini, &
Hoffmeyer, 2012), a lagoon (Collos et al., 2005), and gulfs (D’Agostino et al., 2018).
The heterotrophic bacterial growth could be supported, not only by phytoplankton
exudates, but also by the activity of grazers (Pagano et al., 2006; Peduzzi & Herndl,
1992). Such a microbial loop is very important in coastal environments and could
be involved in active heterotrophic degradation of phytoplankton, as demonstrated